chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5130696139130696140TC27GENICpossibly homozygous55718798
5130696803130696804AG28GENIChomozygous55718802
5130696984130696985TC15GENIChomozygous55896292
5130697030130697034TTAT----5GENIChomozygous55896293
5130697040130697041GT8GENIChomozygous55896294
5130697042130697043TA8GENIChomozygous55896295
5130697128130697129CCT8GENIChomozygous55896296
5130697130130697133TTC---8GENIChomozygous55718804
5130697137130697155TTTCTTTTTTTTTTTTTT------------------7GENIChomozygous55896297
5130698056130698057G-16GENICheterozygous55718808
5130698128130698129TC24GENIChomozygous55896298